IDI1 antibody (AA 31-130) (Biotin)

Catalog No. ABIN709273

This Rabbit Polyclonal antibody specifically detects IDI1 in WB, IHC (p), IP and IHC (fro). It exhibits reactivity toward Human.

Quick Overview for IDI1 antibody (AA 31-130) (Biotin) (ABIN709273)

Target: IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IDI1 antibody is conjugated to Biotin

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunoprecipitation (IP), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-IDI1 Antibody (Biotin)

Binding Specificity: AA 31-130

Purpose: IDI1 Polyclonal Antibody, Biotin Conjugated

Cross-Reactivity: Human, Mouse

Predicted Reactivity: Rat,Cow,Pig,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human IDI1

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000),

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for IDI1

Target: IDI1 (Isopentenyl-Diphosphate delta Isomerase 1 (IDI1))

Alternative Name: IDI1

Background:

Synonyms: IDI1, IPP isomerase 1, IPPI1, Isopentenyl diphosphate Delta isomerase 1, isopentenyl diphosphate dimethylallyl diphosphate isomerase 1, Isopentenyl pyrophosphate isomerase 1, IDI1_HUMAN.

Background: IDI1 is a peroxisomally localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP). These are substrates for the reactions that ultimately result in the synthesis of cholesterol. There is reduction in IPP isomerase activity in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy.

Gene ID: 3422

UniProt: Q13907